Canonical Allele Identifier: CA397460603
Gene: MC1R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89919659T>A , CM000678.2:g.89919659T>A GRCh38
NC_000016.9:g.89986067T>A , CM000678.1:g.89986067T>A GRCh37
NC_000016.8:g.88513568T>A NCBI36
NG_012026.1:g.6781T>A
NG_027810.1:g.2651T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000555147.2:c.401T>A MANE Select ENSP00000451605.1:p.Phe134Tyr
ENST00000639847.1:c.401T>A ENSP00000492011.1:p.Phe134Tyr
ENST00000555147.1:c.401T>A ENSP00000451605.1:p.Phe134Tyr
ENST00000555427.1:c.401T>A ENSP00000451760.1:p.Phe134Tyr
ENST00000556922.1:c.401T>A ENSP00000451560.1:p.Phe134Tyr
NM_002386.3:c.401T>A NP_002377.4:p.Phe134Tyr
NM_002386.4:c.401T>A MANE Select NP_002377.4:p.Phe134Tyr